Liverex I

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Liverex I
Generic name: GINKGO BILOBA, FEL TAURI, GALLBLADDER (SUIS), HEPAR SUIS), THYROIDINUM (SUIS), GERMANIUM SESQUIOXIDE, ALPHA-KETOGLUTARICUM ACIDUM, CITRICUM ACIDUM, FUMARICUM ACIDUM, MALICUM ACIDUM, MANGANUM METALLICUM, PYRUVIC ACID, SUCCINICUM ACIDUM, NAPHTHOCHINONUM, ARSENICUM METALLICUM, SULPHUR, ACONITICUM ACIDUM, CIS, LYCOPODIUM CLAVATUM, NATRUM OXALACETICUM, PHOSPHORUS
Manufacturer: Energique, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 1c23c489-0a43-4736-a30a-0ae02c09fb45
SPL ID: eeacc3c5-b06d-467d-b422-1c9f101149a9
Version: 4
Effective date: 2023-07-21
Source export date: 2026-11-06
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 06:56:02

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 28 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Liverex I	openfda.brand_name
generic name		GINKGO BILOBA, FEL TAURI, GALLBLADDER (SUIS), HEPAR SUIS), THYROIDINUM (SUIS), GERMANIUM SESQUIOXIDE, ALPHA-KETOGLUTARICUM ACIDUM, CITRICUM ACIDUM, FUMARICUM ACIDUM, MALICUM ACIDUM, MANGANUM METALLICUM, PYRUVIC ACID, SUCCINICUM ACIDUM, NAPHTHOCHINONUM, ARSENICUM METALLICUM, SULPHUR, ACONITICUM ACIDUM, CIS, LYCOPODIUM CLAVATUM, NATRUM OXALACETICUM, PHOSPHORUS	openfda.generic_name
manufacturer name		Energique, Inc.	openfda.manufacturer_name
ndc	package	44911-0419-1	openfda.package_ndc
ndc	product	44911-0419	openfda.product_ndc
ndc11	package	44911041901	derived:openfda.package_ndc
spl id		eeacc3c5-b06d-467d-b422-1c9f101149a9	id
spl set id		1c23c489-0a43-4736-a30a-0ae02c09fb45	set_id
unii		27YLU75U4W	openfda.unii
unii		6RV024OAUQ	openfda.unii
unii		8ID597Z82X	openfda.unii
unii		RBF5ZU7R7K	openfda.unii
unii		N712M78A8G	openfda.unii
unii		96WE91N25T	openfda.unii
unii		OF5471ZHRR	openfda.unii
unii		88XHZ13131	openfda.unii
unii		ET3651ZLOU	openfda.unii
unii		42Z2K6ZL8P	openfda.unii
unii		817L1N4CKP	openfda.unii
unii		8558G7RUTR	openfda.unii
unii		70FD1KFU70	openfda.unii
unii		19FUJ2C58T	openfda.unii
unii		XF417D3PSL	openfda.unii
unii		B6A98VOI9I	openfda.unii
unii		6CA025Y4FG	openfda.unii
unii		AB6MNQ6J6L	openfda.unii
unii		6EC706HI7F	openfda.unii
unii		C88X29Y479	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.